Lee’s Santa Dash
09 December 2020
Between the 1st and 25th of December Lee’s aim is to run 100k dressed as Santa on the Isle of Mull! She also has a few elves out and about throughout Mull helping her raise awareness by donning their festive outfits and braving the weather to show their support. As well as raising funds Lee would also like to raise awareness. Mia her daughter was born with Neurofibromatosis Type 1.
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_11_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_8_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_3_800x600.jpg)
![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_16_800x600.jpg)
– Lee"Yup, I hadn’t heard of it either until Mia was diagnosed a few years ago. Mia just gets on with it but there’s no denying it has a massive effect on her life, it can sometimes be really difficult. Very little is known about NF1, even by most health professionals. Nerve Tumours UK provide crucial support to families living with NF1. Without their support, life with NF1 would be even harder. Nerve Tumours UK are campaigning at the moment to raise funds for one more specialist nurse in the UK. I hope to raise funds to help this campaign #OneMoreNurse."
If you want to support and sponsor Lee:
Donate![](/images/common/lee_Paterson_Virtual_Santa_Dash_for_NF_image_1024x768.jpg)
Why not join Lee, grab your Santa/Elf suit and go for a run this December! You can organise yourself as Lee did and set up your own fundraiser or you can sign up to our Virtual Santa Dash which takes place throughout the month of December.
Everyone is welcome! Gather all your friends and family to take on this year’s Christmas challenge, spread joy and happiness to the 26,500 people affected with Neurofibromatosis in the UK.
Filter News
![](https://nervetumours.org.uk/images/made/images/common/Artboard_5_800_600_s_c1.jpg)
Coronavirus and your Mental Health
Mind offers support and advice to help you cope with the impacts of Coronavirus on your mental health and wellbeing.
Read More![](https://nervetumours.org.uk/images/made/images/common/Karen_OneMoreNurse_Mask_Campaign-blackwhite_.37402105_800_600_s_c1.jpg)
2nd Lockdown Announcement
A message from Karen our Charity Director on a 2nd national lockdown - we're here for you
Read More![](https://nervetumours.org.uk/images/made/images/common/Dexter_Parker_370x280_800_600_s_c1.png)
Dexter’s Story
A journey of acceptance with NF1 and understanding that what makes us different from one another is a gift.
Read More![](https://nervetumours.org.uk/images/made/images/common/OneMoreNurse_Mask_Campaign_Website_Header_370x280_800_600_s_c1.png)
#OneMoreNurse
Help support our Campaign, we need your ongoing support now more than ever to continue our vital Specialist NF Network
Read More![](https://nervetumours.org.uk/images/made/images/common/Student_voice_prize_website_header_370x280_800_600_s_c1.png)
#DareToThinkRare
Find out how you can take part in this year's Student Voice Prize 7th annual, international essay competition!
Read More![](https://nervetumours.org.uk/images/made/images/common/global-genes-logo-registered_370x280_800_600_s_c1.png)
RARE Champion of Hope Celebration
Join this years RARE Champion of Hope Awards hosted by Global Genes and be inspired!
Read More![](https://nervetumours.org.uk/images/made/images/common/DSC_0096_London_Marathon_2019_-_Group_photo_preview_website_370x280_800_600_s_c1.png)
A Big “Thanks” for Team Nerve Tumours UK running the London 2020 Marathon!
We want to give a great big thank you to all of you who took part in this year's Virtual London Marathon!
Read More![](https://nervetumours.org.uk/images/made/images/common/NTUK_video_thumbnail_high_res_370x280_800_600_s_c1.png)
How To Use Lipspeakers – Support For Those Affected By Hearing Loss
Frances Harris at Bridge Lipspeaking shares how lipspeaking can help those with hearing loss or total deafness caused by NF2
Read More![](https://nervetumours.org.uk/images/made/images/common/Oxford_University_(Naomis_photo)_370x280_800_600_s_c1.png)
Living with Neurofibromatosis Type 1: An Anthropological Study
Get involved and share your story to help increase cross-cultural understanding and awareness of NF1
Read More